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FDA 510(k)

SUM TAN VI

K-Number: K860144 · 1986-02-12

ApplicantNae, Inc.
Decision Date1986-02-12
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUM TAN VI is the device name listed in this FDA 510(k) record. The listed applicant is Nae, Inc.. It received FDA 510(k) clearance on 1986-02-12 under 510(k) number K860144. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUM TAN VI?

SUM TAN VI is a medical device that received FDA 510(k) clearance on 1986-02-12. The listed applicant is Nae, Inc.. The 510(k) number is K860144.

When did SUM TAN VI receive FDA 510(k) clearance?

SUM TAN VI received FDA 510(k) clearance on 1986-02-12, under 510(k) number K860144.

Who is the listed applicant for SUM TAN VI?

The FDA 510(k) record lists Nae, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUM TAN VI?

The FDA product code for SUM TAN VI is FTC.

Related Devices (Code: FTC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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